Remote Clinical Trials Manager

Merck

Lansing (MI)

Remote

USD 142,000 - 224,000

Full time

4 days ago
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Job summary

Merck in Rahway, USA is seeking a Clinical Research Manager to lead end-to-end project management for assigned protocols in compliance with ICH-GCP, country regulations, and internal policies. This remote-position role may span multiple countries within a cluster and requires strong leadership and cross-functional collaboration.

Responsibilities include acting as primary POC for protocols, driving study deliverables, ensuring quality, coordinating with CRA teams, and managing local risk and

Qualifications

  • 5+ years of experience in clinical research.
  • Bachelor’s degree in science (or comparable).
  • Advanced degree (Master, MD, or PhD) preferred.

Responsibilities

  • Main POC for assigned protocols and links between Country Operations and clinical trial team.
  • Drive and track execution of deliverables to meet country commitments.
  • Ensure compliance with ICH/GCP and country regulations, and internal policies.
  • Review Monitoring Visit Reports and escalate performance issues.
  • Perform quality control visits as required.
  • Lead local study teams and coordinate activities across local country roles.
  • Create and execute local risk management plan for assigned studies.
  • Ensure compliance with CTMS, eTMF, and other systems.
  • Collaborate with outsourcing vendors, investigators, and external partners.
  • Sign contracts and manage budgets where delegated.

Skills

Project management
Leadership
Regulatory understanding
English communication

Education

Bachelor's degree in science

Job description

Merck in Rahway, USA is seeking a Clinical Research Manager to lead end-to-end project management for assigned protocols in compliance with ICH-GCP, country regulations, and internal policies. This remote-position role may span multiple countries within a cluster and requires strong leadership and cross-functional collaboration.

Responsibilities include acting as primary POC for protocols, driving study deliverables, ensuring quality, coordinating with CRA teams, and managing local risk and

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